Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1989 Apr;86(8):2525-9.
doi: 10.1073/pnas.86.8.2525.

Retroviral integration: structure of the initial covalent product and its precursor, and a role for the viral IN protein

Affiliations

Retroviral integration: structure of the initial covalent product and its precursor, and a role for the viral IN protein

P O Brown et al. Proc Natl Acad Sci U S A. 1989 Apr.

Abstract

An essential step in the life cycle of a retrovirus is the integration of a DNA copy of the viral genome into a host cell chromosome. We have analyzed the structure of the initial covalent product of an in vitro retroviral integration reaction and determined the structure of the ends of the unintegrated linear viral DNA molecules present in vivo in cells infected with murine leukemia virus (MLV). Our results lead to the following conclusions: (i) Circularization of viral DNA plays no role in integration. The direct precursor to the integrated MLV provirus is a linear molecule. (ii) The initial step in the integration reaction is probably a cleavage that removes the terminal 2 bases from each 3' end of the viral DNA. This cleavage depends on a virally encoded protein, IN, that has previously been shown genetically to be required for integration. (iii) The resulting viral 3' ends are joined to target DNA to form the initial recombination intermediate.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Annu Rev Genet. 1988;22:77-105 - PubMed
    1. Cell. 1988 Aug 12;54(4):497-504 - PubMed
    1. Proc Natl Acad Sci U S A. 1980 Jul;77(7):3932-6 - PubMed
    1. Gene. 1982 Mar;17(3):271-7 - PubMed
    1. Cell. 1984 Mar;36(3):673-9 - PubMed

Publication types

MeSH terms

LinkOut - more resources